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CHD2 variants are a risk factor for photosensitivity in epilepsy.
Galizia EC, Myers CT, Leu C, de Kovel CG, Afrikanova T, Cordero-Maldonado ML, Martins TG, Jacmin M, Drury S, Krishna Chinthapalli V, Muhle H, Pendziwiat M, Sander T, Ruppert AK, Møller RS, Thiele H, Krause R, Schubert J, Lehesjoki AE, Nürnberg P, Lerche H; EuroEPINOMICS CoGIE Consortium; Palotie A, Coppola A, Striano S, Gaudio LD, Boustred C, Schneider AL, Lench N, Jocic-Jakubi B, Covanis A, Capovilla G, Veggiotti P, Piccioli M, Parisi P, Cantonetti L, Sadleir LG, Mullen SA, Berkovic SF, Stephani U, Helbig I, Crawford AD, Esguerra CV, Kasteleijn-Nolst Trenité DG, Koeleman BP, Mefford HC, Scheffer IE, Sisodiya SM. Galizia EC, et al. Among authors: muhle h. Brain. 2015 May;138(Pt 5):1198-207. doi: 10.1093/brain/awv052. Epub 2015 Mar 17. Brain. 2015. PMID: 25783594 Free PMC article.
Recurrent de novo mutations of SCN1A in severe myoclonic epilepsy of infancy.
Kearney JA, Wiste AK, Stephani U, Trudeau MM, Siegel A, RamachandranNair R, Elterman RD, Muhle H, Reinsdorf J, Shields WD, Meisler MH, Escayg A. Kearney JA, et al. Among authors: muhle h. Pediatr Neurol. 2006 Feb;34(2):116-20. doi: 10.1016/j.pediatrneurol.2005.07.009. Pediatr Neurol. 2006. PMID: 16458823
Association of BRD2 polymorphisms with photoparoxysmal response.
Lorenz S, Taylor KP, Gehrmann A, Becker T, Muhle H, Gresch M, Tauer U, Sander T, Stephani U. Lorenz S, et al. Among authors: muhle h. Neurosci Lett. 2006 May 29;400(1-2):135-9. doi: 10.1016/j.neulet.2006.02.026. Epub 2006 Mar 3. Neurosci Lett. 2006. PMID: 16516380
Nonparalytic poliomyelitis in Lyme borreliosis.
van Baalen A, Muhle H, Straube T, Jansen O, Stephani U. van Baalen A, et al. Among authors: muhle h. Arch Dis Child. 2006 Aug;91(8):660. doi: 10.1136/adc.2006.098392. Arch Dis Child. 2006. PMID: 16861483 Free PMC article. No abstract available.
212 results